His main research concerns Genetics, Bipolar disorder, Internal medicine, Locus and Genotype. His Genetics research focuses on Mutation, Genome-wide association study, Gene, Germline mutation and Linkage disequilibrium. His research integrates issues of Odds ratio and ANK3 in his study of Genome-wide association study.
His Bipolar disorder research includes elements of Schizophrenia, Psychosis, Genetic linkage, Genetic determinism and Single-nucleotide polymorphism. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology, Endocrinology and Oncology. His work in Genotype addresses subjects such as Genetic heterogeneity, which are connected to disciplines such as Nucleic acid amplification technique and Mutation.
His primary areas of study are Genetics, Gene, Internal medicine, Bipolar disorder and Endocrinology. His Genetics study is mostly concerned with Locus, Allele, Mutation, Allele frequency and Genetic variation. His biological study spans a wide range of topics, including Molecular biology and Familial adenomatous polyposis.
His studies deal with areas such as Gastroenterology, Oncology and Genotype as well as Internal medicine. His studies examine the connections between Bipolar disorder and genetics, as well as such issues in Schizophrenia, with regards to Psychosis. His Endocrinology research is multidisciplinary, incorporating elements of Receptor and Platelet.
The scientist’s investigation covers issues in Genetics, Bipolar disorder, Single-nucleotide polymorphism, Genome-wide association study and Internal medicine. His Genetics research focuses on subjects like Schizophrenia, which are linked to Genetic variants. His Bipolar disorder research focuses on Schizophrenia and how it relates to Genomics.
His Single-nucleotide polymorphism study combines topics in areas such as Haplotype, Allele, Allele frequency and Candidate gene. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Odds ratio, Linkage disequilibrium and ANK3. His Internal medicine research includes themes of Gastroenterology, Endocrinology and Oncology.
Peter Propping spends much of his time researching Genetics, Genome-wide association study, Bipolar disorder, Genotype and Single-nucleotide polymorphism. In Genetics, Peter Propping works on issues like Odds ratio, which are connected to SNP. As a part of the same scientific study, Peter Propping usually deals with the Genome-wide association study, concentrating on ANK3 and frequently concerns with Linkage disequilibrium and Psychosis.
His research in Bipolar disorder intersects with topics in Schizophrenia and Case-control study. The concepts of his Single-nucleotide polymorphism study are interwoven with issues in Genetic variation and Allele. His study looks at the relationship between Locus and fields such as Genetic association, as well as how they intersect with chemical problems.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Pamela Sklar;Pamela Sklar;Stephan Ripke;Stephan Ripke;Laura J. Scott;Ole A. Andreassen.
Nature Genetics (2011)
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
Ortrud K. Steinlein;John C. Mulley;Peter Propping;Robyn H. Wallace;Robyn H. Wallace.
Nature Genetics (1995)
A potassium channel mutation in neonatal human epilepsy.
Christian Biervert;Björn C. Schroeder;Christian Kubisch;Samuel F. Berkovic.
Identification of loci associated with schizophrenia by genome-wide association and follow-up
Michael C. O'Donovan;Nicholas Craddock;Nadine Norton;Hywel Williams.
Nature Genetics (2008)
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
A E Baum;N Akula;M Cabanero;I Cardona.
Molecular Psychiatry (2008)
Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers.
E G Jönsson;M M Nöthen;F Grünhage;L Farde.
Molecular Psychiatry (1999)
Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder
Jürgen Deckert;Marco Catalano;Yana V. Syagailo;Monica Bosi.
Human Molecular Genetics (1999)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
Ricardo Segurado;Sevilla D. Detera-Wadleigh;Douglas F. Levinson;Cathryn M. Lewis.
American Journal of Human Genetics (2003)
The electroencephalogram (EEG) as a research tool in human behavior genetics: psychological examinations in healthy males with various inherited EEG variants. I. Rationale of the study. Material. Methods. Heritability of test parameters.
Vogel F;Schalt E;Krüger J;Propping P.
Human Genetics (1979)
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